Efficient degradation of antibiotics by heterojunction photocatalysts driving peroxydisulfate activation under visible light irradiation

被引:13
|
作者
Yang, Qi [1 ,2 ]
Bai, Chang -Wei [3 ]
Sun, Yi-Jiao [3 ]
Liu, Yu-Jie [1 ,2 ]
Hou, Kun-Jie [1 ,2 ]
Chen, Fei [3 ]
机构
[1] Hunan Univ, Coll Environm Sci & Engn, Changsha 410082, Hunan, Peoples R China
[2] Hunan Univ, Key Lab Environm Biol & Pollut Control, Minist Educ, Changsha 410082, Hunan, Peoples R China
[3] Chongqing Univ, Coll Environm & Ecol, Key Lab Three Gorges Reservoir Reg Ecoenvironm, Minist Educ, Chongqing 400045, Peoples R China
关键词
Visible-light-assisted; peroxydisulfate (PDS); Tetracycline; Synergistic effect; ZERO-VALENT IRON; PEROXYMONOSULFATE ACTIVATION; AQUEOUS-SOLUTION; BISPHENOL-A; CARBON DOTS; PERSULFATE; OXIDATION; BI2WO6; KINETICS; REMOVAL;
D O I
10.1016/j.cej.2023.145221
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Heterogeneous iron materials show potential for activating peroxydisulfate (PDS). However, these systems may be constrained by low efficiency and secondary pollution. The visible-light-assisted activation has been demonstrated as a feasible and effective approach to enhance PDS activation by iron-based materials. In this study, a visible-light-responsive Bi2WO6/Fe2O3 heterojunction photocatalyst was synthesized to improve the ability of Fe2O3 for PDS activation through an effective Fe(III)/Fe(II) cycle. Rapid tetracycline (TC, a common antibiotic) removal (91.7% within 60 min at a concentration of 20 mg & BULL;L-1) was achieved in the constructed Bi2WO6/Fe2O3/PDS/vis system under conditions of 0.3 g & BULL;L-1 PDS and 0.3 g & BULL;L-1 catalyst. The corresponding pseudo-first-order rate constant reached 4.16 x 10-2 min-1, which was 8.42 and 16.38 times higher than those of Bi2WO6/Fe2O3/vis and Bi2WO6/Fe2O3/PDS systems, respectively. Moreover, the Bi2WO6/Fe2O3 exhibited favorable stability and reusability even after five cycles. Lastly, a catalytic mechanism for TC removal and PDS activation was proposed based on quenching experiments and electron spin resonance (ESR) tests. The SO4 & BULL;- and & BULL;OH played a major role in TC removal, while & BULL;O2- and 1O2 contributed as auxiliary factors. This study presents a promising strategy for activating PDS using cost-effective and stable Fe(III)-based heterojunctions, and such an idea can be used to design catalysts for other high-value reactions.
引用
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页数:13
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